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Journal article

Glycosylation with Disarmed Glycosyl Bromides Promoted by Iodonium Ions : Glycosylation with Disarmed Glycosyl Bromides Promoted by Iodonium Ions

From

Department of Chemistry, Technical University of Denmark1

Organic Chemistry, Department of Chemistry, Technical University of Denmark2

Iodonium ions have been developed for activating glycosyl bromides in the coupling to glycosyl acceptors. The iodonium ions are generated from N-iodosuccinimide and a protic acid such as camphorsulfonic acid or triflic acid, where the latter gives the most reactive promoter system. The couplings occur with the release of iodine monobromide, and the best results are obtained with benzoylated glycosyl donors and acceptors.

In this way, disarmed glycosyl bromides can serve as glycosyl donors without the use of heavy-metal salts.

Language: English
Year: 2016
Pages: 3119-3125
ISSN: 1434193x and 10990690
Types: Journal article
DOI: 10.1002/ejoc.201600545
ORCIDs: Madsen, Robert

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